Canonical Allele Identifier: CA517479032
Gene: POU3F4 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.82763377C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.83508369C>A , CM000685.2:g.83508369C>A GRCh38
NC_000023.10:g.82763377C>A , CM000685.1:g.82763377C>A GRCh37
NC_000023.9:g.82650033C>A NCBI36
NG_009936.2:g.5109C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000644024.2:c.45C>A MANE Select ENSP00000495996.1:p.Thr15=
ENST00000373200.4:c.45C>A ENSP00000362296.2:p.Thr15=
NM_000307.4:c.45C>A NP_000298.3:p.Thr15=
NM_000307.5:c.45C>A MANE Select NP_000298.3:p.Thr15=
Search 100 bp 5'
Search 100 bp 3'